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7-Hydroxy-1,9-dimethyldibenzo-[B,J]-[1,7]-phenanthroline-8,14-(5H,13H)-dione

Compound with spectra: 1 NMR, 1 FTIR, and 1 MS (GC)

7-Hydroxy-1,9-dimethyldibenzo-[B,J]-[1,7]-phenanthroline-8,14-(5H,13H)-dione
SpectraBase Compound ID 5KEDXA15Zdw
InChI InChI=1S/C22H16N2O3/c1-10-5-3-7-12-16(10)21(26)18-14(23-12)9-15(25)19-20(18)24-13-8-4-6-11(2)17(13)22(19)27/h3-9,25H,1-2H3,(H,23,26)(H,24,27)
InChIKey COKVHPUHRWBQGA-UHFFFAOYSA-N
Mol Weight 356.38 g/mol
Molecular Formula C22H16N2O3
Exact Mass 356.116092 g/mol

View Spectrum of 7-Hydroxy-1,9-dimethyldibenzo-[B,J]-[1,7]-phenanthroline-8,14-(5H,13H)-dione

Vapor Phase IR Spectrum
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View Spectrum of 7-Hydroxy-1,9-dimethyldibenzo-[B,J]-[1,7]-phenanthroline-8,14-(5H,13H)-dione

MS (GC) Spectrum
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum Y-30-1472-32

View Spectrum of 7-Hydroxy-1,9-dimethyldibenzo-[B,J]-[1,7]-phenanthroline-8,14-(5H,13H)-dione

13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • 1,9-Dimethyl-7-oxidanyl-5,13-dihydroquinolino[2,3-c]acridine-8,14-dione
  • 7-Hydroxy-1,9-dimethyl-5,13-dihydroquinolin[2,3-c]acridine-8,14-quinone
  • 7-Hydroxy-1,9-dimethyl-5,13-dihydroquinolino[2,3-c]acridine-8,14-dione
Propyl 4-(2-bromophenyl)-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexahydro-3-quinolinecarboxylate
ISJBDHUGVDBULE-UHFFFAOYSA-N
2-Anthracenecarboxylic acid, 9,10-dihydro-8-hydroxy-3-methoxy-1-methyl-9,10-dioxo-, ethyl ester
1,3-Dioxolo[4,5-b]acridin-10(5H)-one, 11-hydroxy-6-methoxy-5-methyl-
3,6-BISMETHOXYMETHYLBUXIFOLIADINE-H
1,5-Dichlorocyclohepta[def]fluorene-4,8-dione
6-METHOXYNAPHTHO-[1,2-B]-[1-10]PHENANTHROLIN-7-(14H)-ONE
(1'-S)-6-O-METHYL-7-CHLOROAVERANTIN
2H,5H-Pyrano[3,2-c][1]benzopyran-2,5-dione, 4-[3-[(3-chloro-4-fluorophenoxy)methyl]-4-methoxyphenyl]-3,4-dihydro-
1-Acetoxy-2-(2'-acetyl-2'-carbethoxymethyl-3'-oxobutyl)-5-methoxyanthraquinone
Title Journal or Book Year
Natural product chemistry. Part160. Synthesis of 8-, 9-, 10- and 11-methylacronycines to improve the cytostatic activity of acronycine Journal of Heterocyclic Chemistry 1993
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